与年龄相关的肠道屏障完整性损失在胸腺内置和T细胞衰老中起着不可或缺的作用
Jessica Conway1, Erica N De Jong2, Andrea J White3
1Institute of Inflammation and Ageing, University of Birmingham, Birmingham, UK.
Aging cell
|November 15, 2024
概括
老龄化中的肠道屏障功能障碍与免疫系统衰退有关. 这项研究表明,肠道透性增加驱动胸膜衰老和T细胞枯竭,这表明微生物群干预可能促进健康衰老.
科学领域:
- 免疫学 免疫学 免疫学
- 胃肠病学 胃肠病学
- 衰老研究研究 衰老研究
背景情况:
- 肠上皮作为屏障,但功能障碍与衰老和炎症有关.
- 与年龄相关的变化发生在肠道微生物组和胸腺中,但与免疫衰老的直接联系尚未被探索.
研究的目的:
- 调查肠道屏障功能障碍与免疫衰老中的胸膜内变之间的关联.
- 探索肠道屏障完整性对T细胞衰老和全身炎症的影响.
主要方法:
- 分析微生物转移,T细胞种群 (衰老,耗尽,调节) 和老年人胸膜变化.
- 在老化的无菌小鼠中进行的研究,以评估肠道透性在胸膜衰老中的作用.
主要成果:
- 在微生物转移和衰老/耗尽的T细胞之间发现了强烈的关联,在老年人中具有补偿性调节性T细胞扩张.
- 陈旧的无菌小鼠显示出对肠道透性增加的保护,这表明它对胸膜衰老有直接影响.
结论:
- 肠道屏障功能障碍驱动系统性免疫激活和T细胞通过胸腺内置衰老.
- 基于微生物组的干预措施可能会恢复免疫平衡,并促进健康的衰老.
更多相关视频
相关概念视频
T Cell Activation and Clonal Selection
671
T cells are integral to our adaptive immune system, recognizing and effectively responding to foreign antigens. T cell activation and clonal selection are pivotal in orchestrating this immune response. This article elucidates these mechanisms, detailing the roles of cluster of differentiation (CD) markers, major histocompatibility complex (MHC) molecules, costimulatory signals, and the process of clonal selection.
Naive T cells that have not yet encountered an antigen express two primary CD...
Naive T cells that have not yet encountered an antigen express two primary CD...
671
T Cell Types and Functions
954
When T cells with CD4 markers are activated, they give rise to two types of effector cells: helper T cells and regulatory T cells. Meanwhile, T cells with CD8 markers differentiate into effector cytotoxic T cells. The differentiation of CD4 T cells into helper T cell subsets, such as Th1, Th2, and Th17 cells, is dependent on the antigen type, antigen-presenting cell, and regulatory cytokines.
Th1 cells stimulate dendritic cells to express necessary co-stimulatory molecules on their surfaces for...
Th1 cells stimulate dendritic cells to express necessary co-stimulatory molecules on their surfaces for...
954
Renewal of Intestinal Stem Cells
2.5K
The intestinal epithelial lining rapidly renews every 4 to 5 days. The renewal is facilitated by intestinal stem cells (ISCs) located at the base of the crypt– a gland located at the bottom of each villus. ISCs divide asymmetrically to form new stem cells and progenitor daughter cells. The daughter cells are called transit-amplifying (TA) cells which move upwards along the crypt and either differentiate into absorptive cells– the enterocytes or secretory cells– including the...
2.5K
Cells of the Adaptive Immune Response
964
The T and B lymphocytes of the adaptive immune system develop from common lymphoid progenitor cells in the bone marrow. These progenitors give rise to precursors that eventually develop into both T and B lymphocytes. As these precursors mature, they gain the ability to detect and respond to foreign antigens in the body, a process known as immunocompetence. Additionally, these precursors acquire self-tolerance, a process that ensures they do not react to self-antigens. This intricate system...
964
Role Of Notch Signalling In Intestinal Stem Cell Renewal
2.1K
Notch signaling was first discovered in Drosophila melanogaster, where it is involved in cell lineage differentiation. Notch signaling regulates the maintenance and differentiation of intestinal stem cells or ISCs by controlling the expression of atonal homolog 1 or Atoh1. Atoh1 directs cells to differentiate into secretory cells.
Direct cell-to-cell contact is needed for the activation of Notch signaling. The signal is initiated when a notch ligand binds to a receptor on an adjacent cell, also...
Direct cell-to-cell contact is needed for the activation of Notch signaling. The signal is initiated when a notch ligand binds to a receptor on an adjacent cell, also...
2.1K
Cell-mediated Immune Responses
67.2K
Overview
67.2K


